GR00175 | Craniofacial microsomia | HGVRS6235 | 26853712 | - rs13089920 (2.0e-120)
- rs10459648 (1.0e-23)
- rs17802111 (1.0e-17)
- rs11263613 (4.0e-17)
- rs3754648 (5.0e-13)
- rs17090300 (1.0e-11)
- rs7420812 (7.0e-10)
- rs10905359 (5.0e-09)
- rs3923380 (8.0e-08)
- rs754423 (1.0e-07)
- rs4750407 (2.0e-07)
- rs9574113 (8.0e-06)
- rs7222240 (9.0e-06)
- (show allshow less)
| 0.261 | 0.75541 | |
GR00428 | Progressive supranuclear palsy | HGVRS1599 | 21685912 | - rs8070723 (2.0e-118)
- rs1768208 (5.0e-17)
- rs12203592 (6.0e-15)
- rs7571971 (4.0e-13)
- rs1411478 (4.0e-11)
- rs6687758 (6.0e-08)
- rs11568563 (7.0e-08)
- rs6852535 (1.0e-07)
- rs2142991 (3.0e-07)
- (show allshow less)
| 0.377 | 0.806983 | |
GR00114 | Celiac disease | HGVRS849 | 20190752 | - rs2187668 (1.0e-50)
- rs1464510 (3.0e-40)
- rs17810546 (4.0e-28)
- rs13151961 (2.0e-27)
- rs653178 (7.0e-21)
- rs2327832 (4.0e-19)
- rs2816316 (2.0e-17)
- rs13098911 (3.0e-17)
- rs11221332 (5.0e-16)
- rs917997 (1.0e-15)
- rs1738074 (3.0e-15)
- rs802734 (3.0e-14)
- rs13003464 (4.0e-13)
- rs13010713 (5.0e-11)
- rs10903122 (2.0e-10)
- rs1893217 (3.0e-10)
- rs10806425 (4.0e-10)
- rs1250552 (9.0e-10)
- rs4819388 (2.0e-09)
- rs9792269 (3.0e-09)
- rs3748816 (3.0e-09)
- rs13314993 (3.0e-09)
- rs296547 (4.0e-09)
- rs4675374 (6.0e-09)
- rs11712165 (8.0e-09)
- rs17035378 (8.0e-09)
- rs12928822 (3.0e-08)
- rs1033180 (6.0e-08)
- rs5979785 (6.0e-08)
- rs12727642 (9.0e-08)
- rs6691768 (1.0e-07)
- rs6806528 (2.0e-07)
- rs2298428 (2.0e-07)
- rs6974491 (2.0e-07)
- rs4899260 (4.0e-07)
- rs864537 (4.0e-07)
- rs10936599 (5.0e-07)
- rs2762051 (7.0e-07)
- rs2074404 (1.0e-06)
- rs859637 (2.0e-06)
- (show allshow less)
| 0.582 | 0.881337 | |
GR00070 | Black vs. non-black hair color | HGVRS4156 | 26184321 | - rs117322171 (4.0e-09)
- rs16891982 (1.0e-06)
| 0.921 | 0.979717 | |